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- ...into TrackWise. The ideal candidate will bring an understanding of GMP principles, experience in pharmaceutical or dietary supplement... ...Documentation & Audit Support Collaborate with Document Control and QA teams to ensure controlled documents are accurate, current, and...SuggestedTemporary workWork at office
- ...techniques in support of product release, stability and studies in a GMP/GLP laboratory. The role requires hands-on experience with HPLC/... ..., ensuring compliant results and timely collaboration across QA, Manufacturing and R&D teams. #J-18808-Ljbffr PPL Healthcare LLCSuggested
$156.6k - $234.8k
## Associate Director, GMP Operational QualityApplylocations: Boston, MAtime type: Full timeposted on: Posted 8 Days Agojob requisition... ...products internally at Vertex manufacturing facilities.* Manages QA On The Floor and QA Walkthrough programs supporting Vertex GMP...SuggestedWork experience placementSummer workRemote workFlexible hoursDay shift2 days per weekVertex Pharmaceuticals
Boston, MA3 days ago$116k - $174k
...inspection readiness are key to our programs as we advance through the development cycle. The Manager, Quality Assurance, will provide GMP QA oversight for Tango’s CMC development programs and clinical supply activities. This role partners cross-functionally with Technical...SuggestedContract workTango Therapeutics
Boston, MA1 day ago- ...Analyst II to support product release, stability and studies in a GMP/GLP laboratory. The role requires chromatographic proficiency,... ...maintain instrument readiness, document results, and collaborate with QA, Manufacturing, and R&D to meet testing priorities. #J-18808-...Suggested
- Assertio Therapeutics in Lake Forest, Illinois is seeking a QA Manager responsible for overseeing quality aspects related to the manufacture... ...with cGMP regulations. Must have a minimum of 7 years in a GMP environment, with strong communication and risk management skills...SuggestedContract work
$110k - $135k
...Job Description Job Description Description: The Manager, GMP Quality Operations is responsible for day-to-day Quality oversight... ...regulatory submissions (e.g., IND/IMPD and NDA/MAA). Provide QA support for technology transfer and process validation activities...SuggestedLocal areaVIKING THERAPEUTICS INC
San Diego, CA26 days ago- ...Job Description Job Description The GMP Operational Quality Senior Manager is an advanced technical resource in the principles and... ...executes activities on multiple complex projects with emphasis on QA GMP disposition of drug products and devices. Responsibilities...SuggestedContract workShift work
BioPharma Consulting JAD Group
Boston, MA15 days ago - TerrAscend is seeking a QC Technician to support day-to-day quality activities, ensuring GMP-compliant products, materials, and documentation. You’ll partner with Operations, QA, Compliance, and other teams to identify quality concerns, maintain records, and support continuous...Suggested
- ADP, Inc. is seeking a QA Inspector to join its Quality Assurance team in a GMP manufacturing setting. You will inspect packaging finished goods, prepare reports, and ensure compliance with cGMPs, SOPs, and regulatory guidelines. The role requires 2+ years of GMP inspection...SuggestedWork at office
- Lobos Staffing is hiring a QA Associate for a temp-to-perm opportunity in Livermore, CA. The role supports quality and food safety programs while ensuring manufacturing standards comply with FDA, GMP, HACCP, and food safety requirements, and works closely with the QA Manager...SuggestedPermanent employmentTemporary work
- Bright Innovation Labs in New Albany, OH, is seeking a Quality Assurance Inspector to ensure production meets GMP and company standards. You will inspect components, monitor weights and perform tests using standard gauging tools. The role requires strong attention to detail...SuggestedShift workDay shift
$200k - $260k
...LinkedIn and X. We are seeking a Director/Senior Director, GMP Quality Assurance Operations. You will be responsible for providing... ...quality operations keep pace with growing supply demand. Lead QA input into CDMO selection, onboarding, and ongoing management for...SuggestedContract workTemporary workFlexible hoursCrescent Biopharma
Waltham, MAa month ago- Orano Med is hiring a QA Specialist to support GMP manufacturing of raw materials and sterile drugs for clinical trials. You will review documentation, release materials, and help drive quality system improvements. Responsibilities include overseeing sterile processes,...Suggested
- Bachem Americas is seeking a Quality Assurance Specialist III to support real-time batch review, GMP documentation, and QA guidance across sites in a fast-paced manufacturing environment. You will lead audits, improve LEAN GMP processes, review BPRs and validation protocols...Suggested
- ...sector and a Bachelor’s degree or higher. Responsibilities include reviewing batch records, assisting in audits, and ensuring adherence to GMP standards. This role promotes collaboration and strong communication skills in a dynamic team environment. #J-18808-Ljbffr Allakos
- ...Technician with a manufacturing background in aseptic processing within GMP-regulated cleanrooms. You will execute contamination control... ..., and develop compliant protocols while collaborating across QA, regulatory, and manufacturing teams. The role emphasizes precise...
- ...seeks a Quality Assurance Release Specialist responsible for batch disposition and quality system oversight to ensure products meet GMP and regulatory standards before market release. The role involves risk-based decision-making, data evaluation, NCR/CAPA management, and...
- ...Manager, Quality Program Management to lead the integrated quality plan across QA and Quality Systems. This role partners with cross‑functional teams to ensure state of control and compliance with GMP/ISO standards. The ideal candidate will have 8+ years in GMP‑regulated...
$210k - $290k
The Role: The Senior Director, GMP Quality will build/support and maintain fit-for-purpose quality systems, provide independent quality oversight of contract development and manufacturing organizations (CDMOs), contract testing laboratories, and other strategic partners...Contract workFor contractorsShift workGenerate Biomedicines
Somerville, MA2 days ago- American Regent, Inc. in Ohio seeks a Quality Assurance Associate focused on ensuring GMP compliance across packaging lines and inspection rooms. You will perform verifications, AQL inspections, and release of components and materials, while maintaining strict adherence...
- RoslinCT US is seeking an on-site QA Training Specialist to support the training program within the Quality Management System. You will... ...with cross-functional teams to ensure compliance with GMP and QMS standards. Ideal candidates have 3-5 years of pharma/biotech...Work at office
$155k
Lonza is seeking a QA Operations Specialist III to support GMP quality oversight within our biopharmaceutical manufacturing operations. In this role, you will review and approve batch records, logbooks, and supporting documentation, manage deviations and change controls...Lonza
Portsmouth, NHa month ago$155,000 per week
Lonza seeks an LSA QA Sr. Compliance Specialist to ensure GMP and quality compliance within our biopharmaceutical manufacturing environment. In this role, you will provide QA oversight for clinical and commercial operations, reviewing batch records, deviations, CAPAs,...Lonza
Portsmouth, NHa month ago- ...for compliance topics and continuous improvement across quality systems. You will oversee evaluation, implementation, and follow‑up on GMP compliance, investigations, and corrective actions to prevent recurrence. The role reports to the Sr. Director, Quality Assurance and...Temporary work
$159.8k - $239.8k
Job DescriptionThe Associate Director of GMP Operational Quality Assurance is an advanced technical resource and is recognized as an expert... ...events and/or changes for finished goods GMP operationsServe as QA assessor/approver: resolve gaps, approve change plans,...Full timeContract workWork experience placementSummer workVertex Pharmaceuticals
Boston, MA5 days ago- ...Bachelor's Degree in Life Sciences or a related field, with at least 1 year of experience in quality assurance or manufacturing in a GMP environment. Strong attention to detail, project management skills, and proficiency in word processing and spreadsheet tools are essential...
- ...recurring problems and for continuous improvement. Communicates with QA Analysts and QA Assistants and reports any issues/problems to QA... .../slip-resistant shoes, and gloves are required as necessary in accordance with company GMP and safety standards. #J-18808-Ljbffr...Immediate startShift workWeekend work
The Marzetti Company
Columbus, OH2 days ago - ...classoperational excellence.The position ofQA AnalystMaintains and ensures quality of products, collects data, monitors products and processes and GMP compliance. Shift: Monday - Friday 3p - 11:30p with OT as required. Responsibilities Engagement – Marzetti Values: Work Safely,...Monday to FridayShift workWeekend work
The Marzetti Company
Altoona, IA1 day ago - ...of Quality Assurance to lead quality teams and drive a culture where quality is a mindset. You will oversee manufacturing packaging QA, deviations, CAPAs, and change controls, ensuring product quality and patient safety. You will partner cross-functionally and lead continuous...
